A comparison of two different spinal techniques in surgeries below umbilicus.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/071551
- Lead Sponsor
- GMERS Medical College And Hospital Gandhinagar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anaesthesiology (ASA) Grade I & II
weight: 50 – 80 Kgs.
height: 150 – 170 cms
Patients posted for infra-umbilical and lower limb surgery
Exclusion Criteria
Patient refusal for study
Patient with clinically significant Coagulopathy
Patient with spine deformities
Patients with infection at site of Spinal Injection
Patients with associated systemic diseases e.g. hypertension, diabetes mellitus, kidney diseases,
respiratory diseases, cardiovascular diseases, liver disease.
Patients with history of allergy to local anaesthetics and opioids
Pregnant and lactating females
Patients who have history of drug abuse
Psychologically challenged patients
Non cooperative patient
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To compare the intra-operative hemodynamic changes in fractional spinal anaesthesia and <br/ ><br>conventional spinal anaesthesia (Heart Rate, Systolic blood pressure, Diastolic blood pressure, Mean <br/ ><br>Arterial Blood Pressure, SpO2%). <br/ ><br>2. To compare the sensory blockade parameters (time of onset of sensory blockade, time of peak <br/ ><br>level of sensory blockage and duration of sensory blockade) between fractional spinal anaesthesia and <br/ ><br>conventional spinal anaesthesia. <br/ ><br>3. To compare the motor blockade parameters (time of onset of motor blockade, duration of motor <br/ ><br>blockade) between fractional spinal anaesthesia and conventional spinal anaesthesia . <br/ ><br>4. To compare the duration of analgesia between fractional spinal anaesthesia and conventional <br/ ><br>spinal anaesthesia.Timepoint: 2 years
- Secondary Outcome Measures
Name Time Method To study side effects in patients undergoing fractional spinal anaesthesia and conventional spinal <br/ ><br>anaesthesia.Timepoint: 2 years